Multisociety guideline on reprocessing flexible gastrointestinal endoscopes: 2011.

نویسندگان

  • Bret T Petersen
  • Jennifer Chennat
  • Jonathan Cohen
  • Peter B Cotton
  • David A Greenwald
  • Thomas E Kowalski
  • Mary L Krinsky
  • Walter G Park
  • Irving M Pike
  • Joseph Romagnuolo
  • William A Rutala
چکیده

● The beneficial role of GI endoscopy for the prevention, diagnosis, and treatment of many digestive diseases and cancer is well established. Like many sophisticated medical devices, the endoscope is a complex, reusable instrument that requires reprocessing before being used on subsequent patients. The most commonly used methods for reprocessing endoscopes result in high-level disinfection. To date, all published occurrences of pathogen transmission related to GI endoscopy have been associated with failure to follow established cleaning and disinfection/ sterilization guidelines or use of defective equipment. Despite the strong published data regarding the safety of endoscope reprocessing, concern over the potential for pathogen transmission during endoscopy has raised questions about the best methods for disinfection or sterilization of these devices between patient uses. To this end, in 2003, the American Society for Gastrointestinal Endoscopy (ASGE) and the Society for Healthcare Epidemiology of America collaborated with multiple physician and nursing organizations, infection prevention and control organizations, federal and state agencies, and industry leaders to develop evidence-based guidelines for reprocessing GI endoscopes.1,2 Since that ime, high-level disinfectants, automated reprocessing mahines, endoscopes and endoscopic accessories have all volved.3-6 However, the efficacy of decontamination and high-level disinfection is unchanged and the principles guiding both remain valid.7 Additional outbreaks of infection related to suboptimal infection prevention practices during endoscopy or lapses in endoscope reprocessing have been well publicized. A cluster of hepatitis C cases was attributed to grossly inappropriate intravenous medication and sedation practices.8 In numerous other instances, risk of infection transission has been linked to less willful, but incorrect, eprocessing as a result of unfamiliarity with endoscope hannels, accessories, and the specific steps required for eprocessing of attachments.9 Recent on-site ambulatory urgery center surveys confirm widespread gaps in infecion prevention practices.10 Given the ongoing occurrences of endoscopy-associated infections attributed to

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Multisociety guideline on reprocessing flexible GI endoscopes: 2011.

Author(s): Bret T. Petersen, Jennifer Chennat, Jonathan Cohen, Peter B. Cotton, David A. Greenwald, Thomas E. Kowalski, Mary L. Krinsky, Walter G. Park, Irving M. Pike, Joseph Romagnuolo, William A. Rutala Source: Infection Control and Hospital Epidemiology, Vol. 32, No. 6 (June 2011), pp. 527-537 Published by: The University of Chicago Press on behalf of The Society for Healthcare Epidemiology...

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عنوان ژورنال:
  • Gastrointestinal endoscopy

دوره 73 6  شماره 

صفحات  -

تاریخ انتشار 2011